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Completed Not applicable Interventional

Study for Atrial Fibrillation Reduction (SAFARI)

ClinicalTrials.gov ID: NCT00267137

Public ClinicalTrials.gov record NCT00267137. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 1:26 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Atrial fibrillation (AF), which is the name for rapid beats in the upper chambers of the heart, is the world's most common kind of irregular heart beat. People with AF experience symptoms such as heart palpitations (a racing or pounding feeling in the chest), shortness of breath, dizziness, fatigue or weakness. Although AF can occur in otherwise healthy people for no apparent reason, it is sometimes associated with high blood pressure, heart disease or lung problems. The purpose of the SAFARI trial is to study the effectiveness of pacing algorithms in the upper chamber of the heart for patients who have both AF and bradycardia (slow heart beat).

Study identification

NCT ID
NCT00267137
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
540 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2002
Primary completion
Sep 10, 2005
Completion
Jul 20, 2006
Last update posted
Feb 12, 2025

2002 – 2006

United States locations

U.S. sites
34
U.S. states
19
U.S. cities
34
Facility City State ZIP Site status
Not listed Yuma Arizona
Not listed Fayetteville Arkansas
Not listed Fort Smith Arkansas
Not listed Bakersfield California
Not listed Berkeley California
Not listed Los Angeles California
Not listed Aurora Colorado
Not listed Stamford Connecticut
Not listed Clearwater Florida
Not listed Daytona Beach Florida
Not listed Ormond Beach Florida
Not listed Tampa Florida
Not listed Atlanta Georgia
Not listed Chicago Illinois
Not listed Lombard Illinois
Not listed Springfield Illinois
Not listed Shreveport Louisiana
Not listed Brighton Massachusetts
Not listed Lansing Michigan
Not listed Saint Paul Minnesota
Not listed Paterson New Jersey
Not listed Ridgewood New Jersey
Not listed East Syracuse New York
Not listed Rochester New York
Not listed Syracuse New York
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Elyria Ohio
Not listed Pittsburgh Pennsylvania
Not listed Charleston South Carolina
Not listed Nashville Tennessee
Not listed Dallas Texas
Not listed Houston Texas

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00267137, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 12, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00267137 live on ClinicalTrials.gov.

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